US8900265B1 - Clot retrieval system - Google Patents
Clot retrieval system Download PDFInfo
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- US8900265B1 US8900265B1 US14/147,491 US201414147491A US8900265B1 US 8900265 B1 US8900265 B1 US 8900265B1 US 201414147491 A US201414147491 A US 201414147491A US 8900265 B1 US8900265 B1 US 8900265B1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/22—Implements for squeezing-off ulcers or the like on the inside of inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; Calculus removers; Calculus smashing apparatus; Apparatus for removing obstructions in blood vessels, not otherwise provided for
- A61B17/221—Gripping devices in the form of loops or baskets for gripping calculi or similar types of obstructions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00831—Material properties
- A61B2017/00867—Material properties shape memory effect
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/22—Implements for squeezing-off ulcers or the like on the inside of inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; Calculus removers; Calculus smashing apparatus; Apparatus for removing obstructions in blood vessels, not otherwise provided for
- A61B17/221—Gripping devices in the form of loops or baskets for gripping calculi or similar types of obstructions
- A61B2017/2212—Gripping devices in the form of loops or baskets for gripping calculi or similar types of obstructions having a closed distal end, e.g. a loop
Definitions
- the present invention relates to a deployable system for removing a blood clot or other object from a lumen of an animal.
- Acute ischemic strokes develop when a blood clot (thrombus) blocks an artery supplying blood to the brain. Needless to say, when a blood clot creates such a blockage, time in removing the clot is critical.
- intracranial obstructions are limited by several factors, such as the distance of the intracranial obstruction from the femoral access site, the tortuosity (twists and turns in the artery as it enters the base of the skull) of the cervical and proximal intracranial vasculature, the small size of the vessels and the extremely thin walls of intracranial vessels, which lack a significant muscular layer.
- tortuosity tilts and turns in the artery as it enters the base of the skull
- These limitations require a device to be small and flexible enough to navigate through tortuous vessels within a guide catheter and microcatheter, expand after delivery at the site of occlusion and be retrievable into the microcatheter and yet be strong enough to dislodge strongly adherent thrombus from the vessel wall.
- the device should distally entrap or encase the thrombus to prevent embolization to other vessels and to completely remove the occlusion.
- the device should be retrievable without the need for proximal occlusion of the vessel, which carries risk of further ischemia and risk of vessel injury.
- the device should be simple to use and be capable of multi-use within the same patient treatment.
- the device should not be abrasive and should not have sharp corners exposed to the endothelial layer of the vessel wall.
- Currently available devices include the MERCITM RETRIEVER clot retriever device marketed by Concentric Medical, Inc. (Mountainview, Calif.), the PENUMBRATM system marketed by Penumbra Inc. (Alameda, Calif.) to retrieve clots, and the newer stent retrieval devices TREVOTM (Stryker, Kalamazoo, Mich.) and SOLITAIRETM (eV3 Endovascular Inc., Madison, Mass., which is a subsidiary of Covidien). All the devices are ineffectual at removing organized hard thrombus that embolize to the brain from the heart and from atherosclerotic proximal vessels.
- the MERCI retrieval system is comprised of coiled spring-like metal and associated suture material.
- the method of use is deployment distal to the thrombus and by withdrawing the device through the thrombus, the thrombus becomes entangled in the coil and mesh and then is retrieved.
- the MERCI system requires occlusion of the proximal vessel with a balloon catheter and simultaneous aspiration of blood while the thrombus is being removed.
- the device fails to dislodge the thrombus from the wall of the vessel and often, even when successfully dislodging the thrombus, the thrombus embolizes into another or the same vessel due to the open ended nature of the device.
- the next attempt at a thrombus removal system was the PENUMBRA.
- the PENUMBRA is a suction catheter with a separator that macerates the thrombus which is then removed by suction.
- the device is ineffective at removing hard, organized thrombus which has embolized from the heart, cholesterol plaque from proximal feeding arteries and other foreign bodies.
- the SOLITAIRE and TREVO systems are self-expanding non-detachable stents.
- the devices are delivered across the thrombus which is then supposed to become entwined in the mesh of the stent and which is then removed in a manner similar to the MERCI system. Again, these devices are ineffectual at treating hard thrombus.
- the thrombus is often compressed against the vessel wall by the stent which temporarily opens the vessel by outwardly pressing the clot against the vessel wall.
- the clot Upon retrieval of the devices, the clot remains or is broken up into several pieces which embolize to vessels further along the vessel.
- the present disclosure provides a system for removing obstructions and other objects within a blood vessel or other lumen of an animal.
- the system may be deployed in the lumen from a distal end of a catheter and, in some embodiments, includes a pull wire having a proximal end and a distal end; a distal body attached to the pull wire, the distal body comprising an interior, an exterior, a proximal end, a distal end, a plurality of proximal memory metal strips located at the proximal end, a proximal hub located in the distal body interior, and a distal hub located distal relative to the proximal hub.
- the distal body has a relaxed state wherein the distal body has a first height and width and a collapsed state wherein the distal body has a second height and width, the second height less than said first height, the second width less than the first width.
- the system further includes a catheter having an interior, a proximal end leading to the interior and a distal end leading to the interior, the catheter comprised of a biocompatible material and configured to envelope the distal body when the distal body is in the collapsed state.
- Each of the proximal memory metal strips has a proximal end and a distal end and preferably, in the relaxed state, each of the proximal ends of the proximal memory metal strips is located proximal relative to the proximal hub.
- the proximal ends of the proximal memory metal strips are configured to move towards each other and towards the pull wire when an operator moves the proximal hub distally and closer to the stationary distal hub (i.e., when the operator decreases the distance between the hubs).
- the proximal ends of the proximal memory metal strips are configured to move away from each other and away from the pull wire by moving the proximal hub proximally away from the stationary distal hub (i.e., when the operator increases the distance between the hubs).
- the system further includes a plurality of memory metal connector strips, the plurality of memory metal connector strips each having a proximal end attached to a proximal memory metal strip and a distal end attached to the proximal hub.
- the connector strips are integral with the proximal hub (i.e., optionally, the connector strips and the proximal hub are formed from the same piece of memory metal).
- the proximal hub is a tube having an aperture and the pull wire passes through the aperture.
- the proximal hub is slideable along the pull wire (i.e., at least a segment of the pull wire).
- the proximal memory metal strips are distributed substantially evenly about a perimeter of the distal body.
- the distal hub is a tube having an aperture.
- the distal hub is attached to the pull wire such that the distal hub is not slideable along the pull wire.
- the distal body further comprises a lead wire extending distally from the distal hub.
- the distal body comprises a basket comprised of a plurality of memory metal strips distal relative to the proximal memory metal strips.
- the distal hub, the proximal hub, and the distal basket are comprised of a nitinol having the same material composition.
- the distal body further comprises an x-ray marker configured to be detected by an x-ray radiation of 0.01 mrem when the distal body is located in a cranial blood vessel inside the body of a human and the x-ray is taken from outside the human's body.
- the proximal memory metal strips form a claw, the claw having a closeable proximal end formed by the proximal ends of the proximal memory metal strips.
- between 2 and 4 proximal memory metal strips form the claw.
- the distal body in the relaxed state, has a tapered shape in which the distal body height and width decrease from the proximal end to the distal end.
- the distal body in the relaxed state, has a bullet shape.
- the proximal hub and the distal hub are generally cylindrical in shape and each has an outer diameter and an inner diameter that forms the apertures of the proximal and distal hubs, the outer diameters of the proximal and distal hubs are substantially the same size, and the inner diameters of the proximal and distal hubs are substantially the same size.
- the outer diameters of the proximal and distal hubs are from about 0.011 inches to about 0.054 inches, and the inner diameters of the proximal and distal hubs are from about 0.008 inches to about 0.051 inches.
- the pull wire is generally cylindrical and the diameter of the pull wire is between about 0.008 inches and about 0.051 inches.
- the proximal memory metal strips have a length of between about 10 and about 60 millimeters.
- the first height and first width of the distal body are between about 2 millimeters and about 6 millimeters.
- the proximal memory metal strips are configured to a separate a clot from a blood vessel wall.
- the present invention also provides a method of removing an object from an interior lumen of an animal, the lumen having an interior wall forming the lumen.
- the method includes:
- a) providing a system comprising: i) a pull wire having a proximal end and a distal end; ii) a distal body attached to the pull wire, the distal body comprising a proximal end, a distal end, and a claw, the claw comprised of a plurality of memory metal strips, the distal body having a relaxed state wherein the distal body has a first height and width and a collapsed state wherein the distal body has a second height and width, the second height less than said first height, the second width less than said first width; and iii) a catheter having an interior, a proximal end leading to the interior and a distal end leading to the interior, the catheter comprised of a biocompatible material and configured to envelope the distal body when said distal body is in said collapsed state;
- the claw and the memory metal strips are located at the proximal end of said distal body and the distal body is deployed distal to said object.
- the proximal memory metal strips have a proximal end forming the proximal end of the claw and a distal end, and the method includes moving the proximal ends of the memory metal strips towards each other and the pull wire so as to capture the obstruction.
- the distal body further comprises a proximal hub located in the distal body interior, and a distal hub located distal relative to the proximal hub, each of the memory metal strips has a proximal end and a distal end, each of the proximal ends of the memory metal strips is located proximal relative to the proximal hub, and the proximal ends of the memory metal strips are configured to move towards each other and towards the pull wire by moving the proximal hub distally and closer to the distal hub, and the proximal ends of the memory metal strips are configured to move away from each other and away from the pull wire by moving the proximal hub proximally and away from the distal hub, and the method further comprises moving the proximal hub distally and closer to the distal hub so as to capture the obstruction in the claw.
- the interior lumen is an intracranial artery and the obstruction is a blood clot.
- the method further comprises using the clot to move the proximal hub toward the distal hub and exert tension on the proximal memory metal strips.
- the method further comprises using a tube to move the proximal hub toward the distal hub and exert tension on the proximal memory metal strips.
- the present invention also provides a method of manufacturing a system for removing objects within an interior lumen of an animal.
- the method includes:
- proximal tube a middle portion comprising a plurality of memory metal strips attached to the proximal tube and a distal tube;
- proximal segments joining the proximal segments to the distal segments such that the distal segments form the proximal end of a distal body, such that the proximal tube is located inside an interior of said distal body, and such that the proximal tube is located distal relative to the proximal end.
- the method further includes placing a pull wire through the proximal tube such that the proximal tube is slideable along at least a segment of the pull wire.
- the method further includes attaching the pull wire to the distal tube.
- the step of joining the proximal segments to the distal segments comprises welding the proximal segments to the distal segments.
- the proximal end forms a claw comprised of between 2 and 4 memory metal strips, the claw memory metal strips configured to move towards each by moving said proximal tube distally and closer to the distal tube, and the claw memory metal strips configured to move away from each other by moving the proximal tube proximally and away from said distal tube.
- the method further includes not altering the shape of the proximal and distal portions while altering the shape of the middle portion.
- the method further includes cooling the proximal portion, the middle portion, and the distal portion after step D) and, after cooling, the proximal and distal portions have substantially the same size as the proximal and distal portions had prior to step A).
- the method of allowing said middle portion to expand comprises heating the middle portion.
- the method of altering the shape of the middle portion comprises using a mandrel.
- the mandrel is tapered.
- the proximal portion and the distal portion are not cut by the laser.
- the memory metal tube prior to cutting the memory metal tube, has an outer diameter that is from about 0.011 inches to about 0.054 inches and an inner diameter that is from about 0.008 inches to about 0.051 inches.
- FIG. 1A illustrates a side, elevation view of a memory metal tube prior to being cut by a laser.
- FIG. 1B illustrates a side, elevation view of the memory metal tube of FIG. 1A being cut by a laser.
- FIG. 2 a illustrates a side, elevation view of the memory metal tube of FIG. 1B after being cut by a laser; in FIG. 2 a , the tube is shown as though it were flat for purposes of illustrating the cut pattern only.
- FIG. 2 b illustrates a side, perspective view of the memory metal tube of FIG. 1B after being cut by a laser.
- FIG. 2 c illustrates another side, perspective view of the memory metal tube of FIG. 1B after being cut by a laser; in FIG. 2 c , the tube is rotated as compared to FIG. 2 b.
- FIGS. 3A-3H illustrate a method of manufacturing a distal body of one embodiment of the present invention using the laser cut memory metal tube of FIGS. 1 and 2 ; in FIGS. 3A-3H , the basket portion of the distal body is not shown for simplicity of illustration.
- FIGS. 4A-4D illustrate the welding steps of the method of manufacturing shown in FIG. 3 ; in FIGS. 4A-4D , the basket portion of the distal body is not shown for simplicity of illustration.
- FIGS. 5 and 6 illustrate different locations that connector strips may be welded to the proximal memory metal strips.
- FIG. 7 illustrates a side, elevation view of a catheter and the distal body of FIG. 6 .
- FIG. 8 illustrates a side, elevation view of a deployable system of one embodiment of the present invention being used to capture a blood clot; in FIG. 8 , the basket portion of the distal body is not shown for simplicity of illustration.
- FIG. 9 illustrates a side, elevation view of a claw of one embodiment of the present invention being closed by a claw actuator tube; in FIG. 9 , the basket portion of the distal body is not shown for simplicity of illustration.
- FIG. 10 illustrates a side, elevation view of a deployable system of one embodiment of the present invention being used to capture a blood clot; in FIG. 10 , the basket portion of the distal body is not shown for simplicity of illustration.
- the present disclosure provides a deployable system, generally designated by the numeral 10 , for removing an obstruction such as a blood clot 12 or other object from a blood vessel 14 or other interior lumen of an animal.
- the obstruction may be, for example, extruded coils during aneurysm treatment, intravascular embolic material such as onyx or other obstructions requiring mechanical intravascular removal from small distal vessels.
- the drawings not all reference numbers are included in each drawing for the sake of clarity.
- the deployable system 10 includes a pull wire 16 that has a proximal end (not shown) and a distal end 20 .
- the diameter of the pull wire is between about 0.008 inches and about 0.051 inches.
- the system 10 further includes a distal body 22 , which is attached to the pull wire 16 .
- the distal body 22 has a proximal end 24 , a distal end 26 , an interior 28 , and an exterior 30 .
- the distal body 22 has a collapsed state, wherein the distal body 22 has a first height and width and is configured to fit into a catheter 50 (see FIG. 10A ), and a relaxed state wherein the distal body 22 has a different height 32 and width and is configured to expand to about the height and width of a human blood vessel 14 when the distal body 22 is deployed from the catheter 50 (see FIGS. 10B-G ).
- the distal body 22 further includes a proximal hub 74 and a distal hub 76 that is located distal relative to the proximal hub 74 .
- the distal body 22 includes a plurality of strips 40 comprised of a memory metal (e.g., a memory metal alloy such as nitinol) that form the proximal end 24 of the distal body 22 .
- the proximal memory metal strips 40 each have a distal end 44 and a proximal end 42 that forms an openable and closeable claw 46 .
- the proximal memory metal strips 40 are attached to the proximal hub 74 through connector memory metal strips 48 .
- the proximal hub 74 may be slideable along at least a segment of the pull wire 16 , in contrast to the distal hub 76 , which is optionally fixed to the pull wire 16 and not slideable along the pull wire 16 .
- Moving the proximal hub 74 distally and closer to the distal hub 76 i.e., shortening the distance 88 between the proximal hub 74 and distal hub 76 by moving the proximal hub 74 distally while keeping the distal hub 76 stationary
- This tension causes the proximal ends 42 of the proximal memory metal strips 40 to move radially toward each other and the pull wire 16 .
- the claw 46 formed by the proximal memory metal strips 40 ) is brought from the open position to at least a partially closed position, which in turn, separates the obstruction 12 from the wall of the human lumen 14 and captures the obstruction 12 . See FIG. 3H , FIG. 8 , FIG. 9F , and FIGS. 10F and 10G .
- proximal hub 74 moves proximally and away from the distal hub 76 (i.e., increasing the distance 88 between the hubs 74 and 76 ) releases the tension in the proximal memory metal strips 40 , which in turn, causes the proximal ends 42 of the proximal memory metal strips 40 to move away from each other and the pull wire 16 , opening the claw 46 .
- the claw 46 and proximal hub 74 form several functions. First, as described, closing of the claw 46 captures the obstruction 12 . Second, closing the claw 46 retracts the claw 46 from the wall of the lumen 14 so that the claw 46 does not scrape against (and damage) the lumen wall while capturing the obstruction 12 .
- closing the claw 46 reduces the height and width of the distal body 22 , which allows the distal body 22 to be re-sheathed in the catheter 50 , which may be desired, for example, if the operator seeks to re-deploy the distal body 22 in another location in the body (which may be the case if the operator originally deploys the distal body 22 in the wrong location in the lumen 14 ).
- “closing the claw” embraces both partially closing the claw 46 (where the proximal ends 42 of the proximal memory metal strips 40 do not contact the pull wire 16 ) and fully closing the claw 46 (where the proximal ends 42 contact the pull wire 16 ).
- the claw 46 may be comprised of any number of proximal memory metal strips 40 .
- proximal memory metal strips 40 comprise the claw 46 (it being understood that the connector strips 48 , if present, merely serve to tether the claw 46 to the proximal hub 74 ).
- the proximal memory metal strips 40 have a length of between about 10 and about 60 millimeters. The proximal memory metal strips 40 can be thought of as arms of the claw 46 .
- the connector strips 48 are integral with the proximal hub 74 (i.e., formed from the same piece of memory metal). In other embodiments, the proximal hub 74 may be welded to the connector strips 48 .
- the proximal memory metal strips 42 are distributed substantially evenly about a perimeter of the distal body 22 .
- the distal body 22 includes a lead wire 52 extending distally from the distal body 22 .
- the lead wire 52 extends distally from the distal hub 76 . If present, the lead wire 52 may be used to facilitate movement of the system 10 in the lumen 14 .
- the distal body 22 includes a basket 54 distal to the proximal memory metal strips 40 , the basket 54 comprised of a plurality of memory metal strips 56 distal relative to the proximal memory metal strips 40 .
- the distal memory metal strips 56 may, for example, form a basket 54 with a plurality of mesh openings 58 .
- the size of the mesh openings 58 in the basket 54 when the distal body 22 is in its relaxed state is less (preferably significantly less) than the diameter of an average-sized ischemic blood clot 12 so that the blood clot 12 does not escape from the distal basket 54 after being captured by the distal body 22 .
- the basket 54 has an open proximal end 60 and a substantially closed distal end 62 , which is formed by distal tube 76 .
- the distal and proximal hubs 74 and 76 and the distal basket 54 are comprised of a nitinol having the same material composition.
- the size of the mesh openings 58 decreases from the proximal end 60 of the basket 54 to the distal end 62 .
- the distal basket 54 is best seen in FIG. 2 and can be comprised of a different number of cell patterns.
- the distal basket 54 is not shown in FIGS. 3-10 for ease of illustrating the other components in the system 10 .
- the proximal hub 74 and the distal hub 76 are cylindrical tubes comprising substantially circular apertures that span the length of the hubs 74 and 76 and the hubs 74 and 76 have approximately the same inner diameter 72 and the same outer diameter 70 .
- the inner diameter 72 is at least slightly larger than the diameter of the pull wire 16 so that the pull wire 16 can slide through the proximal hub 74 .
- the outer diameters 70 of the proximal and distal hubs 74 and 76 may be from about 0.011 inches to about 0.054 inches and the inner diameters 72 of the proximal and distal hubs 74 and 76 may be from about 0.008 inches to about 0.051 inches.
- the distal body 22 further comprises an x-ray marker 64 configured to be detected by an x-ray radiation of 0.01 mrem when the distal body 22 is located in a cranial blood vessel inside the body of a human and the x-ray is taken from outside the human's body.
- the x-ray markers 64 may be, for example, located at the welding site. In some cases, the increased thickness at the welding site may in of itself comprise the x-ray marker 64 .
- the term “catheter” generally refers to any suitable tube through which the system 10 can be deployed.
- the catheter 50 is sterile and comprised of a biocompatible material (i.e., a material that does not irritate the human body during the course of a 45 minute operation that involves using the system 10 to remove a clot 12 from an intracranial blood vessel 14 ).
- the catheter 50 can be any suitable shape, including but not limited to generally cylindrical.
- the catheter 50 is a microcatheter.
- the catheter 50 envelopes the system 10
- the catheter 50 envelopes at least one component of the system 10 (preferably, the distal body 22 , the lead wire 52 , and the pull wire 16 ).
- the catheter 50 is about 2.5 French in diameter.
- the catheter 50 is delivered to the region of the lumen 14 that has the obstruction 12 as follows: a guide wire is delivered to the obstruction region past the obstruction 12 ; the catheter 50 is delivered over the guide wire; the guide wire is removed; and the system 10 is delivered with its pull wire 16 and lead wire 52 through the catheter 50 .
- the pull wire 16 is used to push the system 10 through the catheter 50 as well as to retrieve the distal body 22 after capturing the obstruction 14 as described below.
- the system 10 may utilize a plurality of catheters 50 , such as, for example, a wider catheter that travels to the brain and a very flexible, smaller diameter microcatheter that is delivered from the first catheter and travels through the small arteries of the brain.
- the distal body 22 or optionally just the distal basket 54 has a tapered shape (e.g., substantially conical or bullet in shape) so that the distal body 22 or just the distal basket 54 tapers from the distal body 22 or the distal basket's 54 proximal end to the distal end.
- a tapered shape e.g., substantially conical or bullet in shape
- the proximal end of the system 10 is shown at the left end of FIGS. 1 and 3 - 10 and the distal end of the system 10 is shown at the right end of FIGS. 1 and 3 - 10 because a principal use of the system 10 is to remove a blood clot 12 from a human intracranial artery 14 , in which case the system 10 generally will enter the artery 14 at its proximal end by the surgeon entering the patient's body near the groin and pushing the catheter 50 towards the brain.
- the diameter of human arteries 14 generally decrease from their proximal end to their distal end.
- the distal body 22 may be located proximally relative to the catheter 50 as the term proximally and distally are used in that lumen.
- the surgeon may deploy the distal body 22 by, for example, moving the catheter 50 proximally so as to unsheathe the distal body 22 or by pushing the distal body 22 out of the catheter 50 .
- a catheter 50 which contains the collapsed distal body 22 is positioned in the lumen 14 distal to the clot 12 . See FIG. 10A .
- the distal body 22 is deployed from the catheter 50 and the height and width of the distal body 22 expand to about the height and width of the blood vessel 14 . See FIG. 10B .
- the catheter 50 is pulled proximally and a claw-actuator tube 90 is deployed into the blood vessel 14 . See FIG. 10C .
- the distal body 22 is moved proximally so that the clot 12 is located in the interior 28 of the distal body 22 . See FIGS. 10D and 10E .
- the claw-actuator tube 90 is moved distally, which pushes the proximal hub 74 distally so that the distance 88 between the proximal hub 74 and the distal hub 76 (which is fixed to the pull wire 16 and kept stationary) decreases. Distal movement of the proximal hub 74 exerts tension on the connector and proximal memory metal strips 40 and 48 , which in turn, closes the claw 46 . See FIG. 10F .
- the claw actuator tube 90 should float on the pull wire 16 —i.e., have an aperture extending the tube's length that has a diameter larger than the diameter of the pull wire 16 —and the aperture of the claw actuator tube 90 should be smaller than the diameter of the proximal hub 74 so that the claw actuator tube 90 pushes the proximal hub 74 ).
- the system 10 is withdrawn proximally and removed from the body. See FIG. 10G .
- a distal body 22 with a distal basket 54 , proximal and distal hubs 74 and 76 , and a claw 46 comprised of three proximal memory metal strips 42 was tested in a flow model that included a tube and a moist cotton ball located in the tube.
- the cotton ball was used to simulate a blood clot.
- the system 10 was deployed distal to the cotton ball.
- the claw 46 was closed by moving the proximal hub 74 distally to capture the cotton ball.
- the system 10 and cotton ball were withdrawn proximally in the tube.
- the distal body 22 is prepared by a process that includes one or more of the following steps, as illustrated in FIGS. 1-4
- the method further includes placing the pull wire 16 through the proximal tube 74 so that the proximal tube 74 is slideable along at least a segment of the pull wire 16 .
- the method further includes attaching the pull wire 16 to the distal tube 76 so that the distal tube 76 is not slideable along the pull wire 16 but instead the distal tube 76 moves with the pull wire 16 .
- the proximal end 24 of the distal body 22 forms a claw 46 comprised of between 2 to 4 proximal memory metal strips 40 , the claw proximal memory metal strips 40 configured to move towards each other and the pull wire 16 by moving the proximal tube 74 distally and toward the distal tube 76 (i.e., decreasing the distance 88 between the tubes 74 and 76 ) and the claw memory metal strips 40 configured to move away from each other and away from the pull wire (i.e., increasing the distance 88 between the tubes 74 and 76 ) by moving the proximal tube 76 proximally and away from the distal tube 76 (as described previously).
- the middle portion 78 is expanded by heating the mandrel and the middle portion 78 by, for example, placing the mandrel and the middle portion 78 in a fluidized sand bath at about 500° C. for about 3 to about 7 minutes. As the middle portion 78 is heated, the heating causes the crystalline structure of the memory metal tube 68 to realign.
- the mandrel is tapered (e.g., substantially conical or bullet in shape) so that the distal basket 54 formed from the middle portion 78 tapers from the proximal end 60 to the distal end 62 .
- the proximal and distal ends of the tube 74 and 76 are not shape set by the mandrel and are not cut by the laser 80 so that the proximal and distal ends 74 and 76 do not change in shape and only slightly expand in size under heating and return to the size of the native tube 68 after the heat is removed.
- the laser cuts are programmed via a computer.
- the laser 80 is preferably focused between the inner and outer diameter of the desired cutting surface and a coolant is passed through the memory metal tube 68 so that the laser 80 cools before reaching the surface directly opposite the desired cutting surface.
- the portions of the wall not cut by the laser 80 create the distal basket 53 , proximal and distal tubes 74 and 76 , and memory metal strips 40 , 48 and 56 , as described.
- the memory metal selected for the native tube 68 has a heat of transformation below average human body temperature (37° C.) so that the distal body 22 has sufficient spring and flexibility after deployment from the catheter 50 in the human blood vessel 14 .
- the native tube 68 (and hence the distal and proximal tubes 74 and 76 ) have an outer diameter of less than about 4 French, e.g., a diameter of about 1 to about 4 French.
- the diameter of the pull wire 16 is between about 0.008 inches and about 0.051, as noted above, and in such embodiments, the diameter of the pull wire 16 may be approximately equal to the inner diameter 72 of the native nitinol tube 68 .
- manufacturing the distal body 22 from a single memory metal tube 68 provides ease of manufacturing and safety from mechanical failure and provides tensile strength necessary for the system 10 to remove hard thrombus 12 and other obstructions.
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Abstract
Description
b) cutting the wall of the
c) removing the pieces of the
d) altering the shape of the
e) quenching the
f) removing the mandrel from the middle portion 78 (see
g) mechanically or chemically electropolishing the
h) cutting the memory metal strips 82 to form a
i) joining the proximal segments to the distal segments such that the distal segments form the proximal end 24 of the
Claims (30)
Priority Applications (26)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/147,491 US8900265B1 (en) | 2014-01-03 | 2014-01-03 | Clot retrieval system |
US14/558,705 US9173668B2 (en) | 2014-01-03 | 2014-12-02 | Clot retrieval system |
US14/558,712 US9155552B2 (en) | 2014-01-03 | 2014-12-02 | Clot retrieval system |
PCT/US2015/010178 WO2015103547A1 (en) | 2014-01-03 | 2015-01-05 | Clot retrieval system |
US14/794,783 US9962177B2 (en) | 2014-01-03 | 2015-07-08 | Clot retrieval system |
US15/158,137 US9566412B2 (en) | 2014-01-03 | 2016-05-18 | Method of manufacturing a catheter-delivered medical device from a tube |
US15/374,307 US9839506B2 (en) | 2014-01-03 | 2016-12-09 | Catheter-delivered endovascualar devices |
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US16/579,427 US20200015831A1 (en) | 2014-01-03 | 2019-09-23 | Clot retrieval system |
US17/075,304 US11160572B2 (en) | 2014-01-03 | 2020-10-20 | Clot retrieval system |
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